Cholinergic regulation of cortical development and plasticity. New twists to an old story.

C F Hohmann, J Berger-Sweeney
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Abstract

Cholinergic afferents innervate cerebral cortex during the most dynamic period of neuronal differentiation and synapse formation, suggesting they play a possible regulatory role in these events. A number of in vivo studies have shown over the last decade that alterations in cholinergic innervation during early postnatal development can change various features of cortical ontogeny. In particular, neonatal lesions to basal forebrain cholinergic afferents result in delayed cortical neuronal development and permanently altered cortical cytoarchitecture and cognitive behaviors. Likewise, cholinergic manipulations affect morphological plasticity in cat visual cortex as well as in the somatosensory cortex of rodents. Furthermore, augmentation of cholinergic function by means of perinatal choline treatment enhances cognitive performance in a sex specific manner. Additional indications for a sexual dimorphism in cortical cholinergic innervation and resulting function are gathered from a variety of paradigms. Recent information about effects of NGF, BDNF and NTB-4/5 on cortical morphogenesis and plasticity reveals complex interactions between the cholinergic basal forebrain afferents and this neurotrophin family. Detailed studies on the expression of cholinergic receptor proteins in cortical development and their associated signal transduction pathways strongly point towards a morphogenetic function of muscarinic receptors, in particular. Transient receptor localization in thalamocortical terminal fields and on a variety of other non-cholinergic fiber bundles suggest a cholinergic role in target finding and/or synapse formation for cortical afferents and efferents. We propose a hypothesis regarding the mechanisms for cholinergic regulation of neuronal differentiation and synapse formation on the level of the individual growth cone and discuss possibilities for cholinergic interactions with differential gene expression. We conclude that understanding the precise role of the cholinergic system in cortical morphogenesis and its relationship to neurotrophin function will be of clinical relevance for a number of developmental brain disorders, including Down Syndrome and Rett Syndrome.

胆碱能调节皮质发育和可塑性。老故事的新转折。
胆碱能传入事件在神经元分化和突触形成最活跃的时期支配大脑皮层,表明它们可能在这些事件中起调节作用。在过去的十年中,许多体内研究表明,出生后早期发育过程中胆碱能神经支配的改变可以改变皮层个体发育的各种特征。特别是,新生儿基底前脑胆碱能传入损伤导致皮质神经元发育延迟和皮质细胞结构和认知行为永久改变。同样,胆碱能操作影响猫视觉皮层和啮齿动物体感觉皮层的形态可塑性。此外,通过围产期胆碱治疗增强胆碱能功能,以性别特定的方式增强认知表现。皮质胆碱能神经支配和由此产生的功能的性二态性的其他适应症从各种范式中收集。最近关于NGF、BDNF和ntc -4/5对皮质形态发生和可塑性影响的研究表明,胆碱能基底前脑传入神经与ntc -4/5神经营养蛋白家族之间存在复杂的相互作用。对皮质发育中胆碱能受体蛋白表达及其相关信号转导途径的详细研究强烈指出,尤其是毒蕈碱受体的形态发生功能。瞬时受体定位于丘脑皮质末端场和多种其他非胆碱能纤维束,表明胆碱能在皮层传入和传出的目标发现和/或突触形成中起作用。我们提出了一个关于胆碱能在个体生长锥水平上调控神经元分化和突触形成的机制的假设,并讨论了胆碱能与差异基因表达相互作用的可能性。我们的结论是,了解胆碱能系统在皮层形态发生中的确切作用及其与神经营养因子功能的关系,将对许多发育性脑疾病,包括唐氏综合征和Rett综合征具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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